Literature DB >> 23281921

Alt Event Finder: a tool for extracting alternative splicing events from RNA-seq data.

Ao Zhou1, Marcus R Breese, Yangyang Hao, Howard J Edenberg, Lang Li, Todd C Skaar, Yunlong Liu.   

Abstract

BACKGROUND: Alternative splicing increases proteome diversity by expressing multiple gene isoforms that often differ in function. Identifying alternative splicing events from RNA-seq experiments is important for understanding the diversity of transcripts and for investigating the regulation of splicing.
RESULTS: We developed Alt Event Finder, a tool for identifying novel splicing events by using transcript annotation derived from genome-guided construction tools, such as Cufflinks and Scripture. With a proper combination of alignment and transcript reconstruction tools, Alt Event Finder is capable of identifying novel splicing events in the human genome. We further applied Alt Event Finder on a set of RNA-seq data from rat liver tissues, and identified dozens of novel cassette exon events whose splicing patterns changed after extensive alcohol exposure.
CONCLUSIONS: Alt Event Finder is capable of identifying de novo splicing events from data-driven transcript annotation, and is a useful tool for studying splicing regulation.

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Year:  2012        PMID: 23281921      PMCID: PMC3535697          DOI: 10.1186/1471-2164-13-S8-S10

Source DB:  PubMed          Journal:  BMC Genomics        ISSN: 1471-2164            Impact factor:   3.969


  22 in total

1.  EST comparison indicates 38% of human mRNAs contain possible alternative splice forms.

Authors:  D Brett; J Hanke; G Lehmann; S Haase; S Delbrück; S Krueger; J Reich; P Bork
Journal:  FEBS Lett       Date:  2000-05-26       Impact factor: 4.124

2.  Alternative splicing and genome complexity.

Authors:  David Brett; Heike Pospisil; Juan Valcárcel; Jens Reich; Peer Bork
Journal:  Nat Genet       Date:  2001-12-17       Impact factor: 38.330

3.  A genomic view of alternative splicing.

Authors:  Barmak Modrek; Christopher Lee
Journal:  Nat Genet       Date:  2002-01       Impact factor: 38.330

4.  The human genome browser at UCSC.

Authors:  W James Kent; Charles W Sugnet; Terrence S Furey; Krishna M Roskin; Tom H Pringle; Alan M Zahler; David Haussler
Journal:  Genome Res       Date:  2002-06       Impact factor: 9.043

Review 5.  Alternative splicing: new insights from global analyses.

Authors:  Benjamin J Blencowe
Journal:  Cell       Date:  2006-07-14       Impact factor: 41.582

6.  Alternative splicing in disease and therapy.

Authors:  Mariano A Garcia-Blanco; Andrew P Baraniak; Erika L Lasda
Journal:  Nat Biotechnol       Date:  2004-05       Impact factor: 54.908

7.  Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation.

Authors:  Cole Trapnell; Brian A Williams; Geo Pertea; Ali Mortazavi; Gordon Kwan; Marijke J van Baren; Steven L Salzberg; Barbara J Wold; Lior Pachter
Journal:  Nat Biotechnol       Date:  2010-05-02       Impact factor: 54.908

8.  Annotating genomes with massive-scale RNA sequencing.

Authors:  France Denoeud; Jean-Marc Aury; Corinne Da Silva; Benjamin Noel; Odile Rogier; Massimo Delledonne; Michele Morgante; Giorgio Valle; Patrick Wincker; Claude Scarpelli; Olivier Jaillon; François Artiguenave
Journal:  Genome Biol       Date:  2008-12-16       Impact factor: 13.583

9.  Alternative isoform regulation in human tissue transcriptomes.

Authors:  Eric T Wang; Rickard Sandberg; Shujun Luo; Irina Khrebtukova; Lu Zhang; Christine Mayr; Stephen F Kingsmore; Gary P Schroth; Christopher B Burge
Journal:  Nature       Date:  2008-11-27       Impact factor: 49.962

10.  Variation in alternative splicing across human tissues.

Authors:  Gene Yeo; Dirk Holste; Gabriel Kreiman; Christopher B Burge
Journal:  Genome Biol       Date:  2004-09-13       Impact factor: 13.583

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  11 in total

1.  Prp8 impacts cryptic but not alternative splicing frequency.

Authors:  Megan Mayerle; Samira Yitiz; Cameron Soulette; Lucero E Rogel; Andrea Ramirez; J Matthew Ragle; Sol Katzman; Christine Guthrie; Alan M Zahler
Journal:  Proc Natl Acad Sci U S A       Date:  2019-01-23       Impact factor: 11.205

Review 2.  A survey of computational methods in transcriptome-wide alternative splicing analysis.

Authors:  Jianbo Wang; Zhenqing Ye; Tim H-M Huang; Huidong Shi; Victor Jin
Journal:  Biomol Concepts       Date:  2015-03

3.  Revealing Missing Human Protein Isoforms Based on Ab Initio Prediction, RNA-seq and Proteomics.

Authors:  Zhiqiang Hu; Hamish S Scott; Guangrong Qin; Guangyong Zheng; Xixia Chu; Lu Xie; David L Adelson; Bergithe E Oftedal; Parvathy Venugopal; Milena Babic; Christopher N Hahn; Bing Zhang; Xiaojing Wang; Nan Li; Chaochun Wei
Journal:  Sci Rep       Date:  2015-07-09       Impact factor: 4.379

4.  spliceR: an R package for classification of alternative splicing and prediction of coding potential from RNA-seq data.

Authors:  Kristoffer Vitting-Seerup; Bo Torben Porse; Albin Sandelin; Johannes Waage
Journal:  BMC Bioinformatics       Date:  2014-03-23       Impact factor: 3.169

5.  Read-Split-Run: an improved bioinformatics pipeline for identification of genome-wide non-canonical spliced regions using RNA-Seq data.

Authors:  Yongsheng Bai; Jeff Kinne; Brandon Donham; Feng Jiang; Lizhong Ding; Justin R Hassler; Randal J Kaufman
Journal:  BMC Genomics       Date:  2016-08-22       Impact factor: 3.969

6.  Alternative Splicing within and between Drosophila Species, Sexes, Tissues, and Developmental Stages.

Authors:  Lauren Gibilisco; Qi Zhou; Shivani Mahajan; Doris Bachtrog
Journal:  PLoS Genet       Date:  2016-12-09       Impact factor: 5.917

Review 7.  Comparison of Alternative Splicing Junction Detection Tools Using RNA-Seq Data.

Authors:  Lizhong Ding; Ethan Rath; Yongsheng Bai
Journal:  Curr Genomics       Date:  2017-06       Impact factor: 2.236

8.  Genomics in 2012: challenges and opportunities in the next generation sequencing era.

Authors:  Zhongming Zhao; Yufei Huang; Bing Zhang; Yu Shyr; Hua Xu
Journal:  BMC Genomics       Date:  2012-12-17       Impact factor: 3.969

9.  Novel bioinformatics method for identification of genome-wide non-canonical spliced regions using RNA-Seq data.

Authors:  Yongsheng Bai; Justin Hassler; Ahdad Ziyar; Philip Li; Zachary Wright; Rajasree Menon; Gilbert S Omenn; James D Cavalcoli; Randal J Kaufman; Maureen A Sartor
Journal:  PLoS One       Date:  2014-07-03       Impact factor: 3.240

10.  ISOexpresso: a web-based platform for isoform-level expression analysis in human cancer.

Authors:  In Seok Yang; Hyeonju Son; Sora Kim; Sangwoo Kim
Journal:  BMC Genomics       Date:  2016-08-12       Impact factor: 3.969

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